Canonical Allele Identifier: CA349336683

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175614817T>A (hg19) ; chr2:g.174750089T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750089T>A , CM000664.2:g.174750089T>A	GRCh38
NC_000002.11:g.175614817T>A , CM000664.1:g.175614817T>A	GRCh37
NC_000002.10:g.175323063T>A	NCBI36
NG_008172.1:g.19384A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.370A>T	ENSP00000490338.2:p.Thr124Ser
ENST00000672640.1:c.370A>T	ENSP00000500507.1:p.Thr124Ser
ENST00000261007.9:c.934A>T	ENSP00000261007.5:p.Thr312Ser
ENST00000348749.9:c.859A>T MANE Select	ENSP00000261008.5:p.Thr287Ser
ENST00000409219.5:c.859A>T	ENSP00000386611.1:p.Thr287Ser
ENST00000409542.5:c.613A>T	ENSP00000387026.1:p.Thr205Ser
ENST00000435083.5:c.*503A>T	ENSP00000395805.1:n.*503A>T
NM_000079.3:c.859A>T	NP_000070.1:p.Thr287Ser
NM_001039523.2:c.934A>T	NP_001034612.1:p.Thr312Ser
XM_017003256.1:c.955A>T	XP_016858745.1:p.Thr319Ser
XM_017003257.1:c.880A>T	XP_016858746.1:p.Thr294Ser
NM_000079.4:c.859A>T MANE Select	NP_000070.1:p.Thr287Ser
NM_001039523.3:c.934A>T	NP_001034612.1:p.Thr312Ser